Ludovic Jeanson

945 total citations
5 papers, 292 citations indexed

About

Ludovic Jeanson is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Ludovic Jeanson has authored 5 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pulmonary and Respiratory Medicine, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Ludovic Jeanson's work include Cystic Fibrosis Research Advances (4 papers), Genetic and Kidney Cyst Diseases (3 papers) and Protist diversity and phylogeny (2 papers). Ludovic Jeanson is often cited by papers focused on Cystic Fibrosis Research Advances (4 papers), Genetic and Kidney Cyst Diseases (3 papers) and Protist diversity and phylogeny (2 papers). Ludovic Jeanson collaborates with scholars based in France, Switzerland and Belgium. Ludovic Jeanson's co-authors include Estelle Escudier, A. Coste, Jean‐François Papon, Serge Amselem, Philippe Duquesnoy, Bruno Copin, Marie Legendre, Guy Montantin, Annick Clément and Esther Kott and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Journal of Proteome Research.

In The Last Decade

Ludovic Jeanson

5 papers receiving 292 citations

Peers

Ludovic Jeanson

GENET

MB

PRM

RM

PHEOH

Isabella Aprea Germany

Esther Kott France

Inga M. Höben Germany

Rathi D. Thiagarajan Australia

Zeineb Bakey Germany

Silvia E. Racedo United States

Alina Wojda Poland

Thassadite Dirami France

Shirley R. Bruce United States

Francesca Cioppi Italy

Isabella Aprea Germany

Ludovic Jeanson

143 ×0.9

GENET

89 ×0.6

MB

99 ×0.8

PRM

39 ×1.0

RM

32 ×0.9

PHEOH

Citations per year, relative to Ludovic Jeanson Ludovic Jeanson (= 1×) peers Isabella Aprea

Countries citing papers authored by Ludovic Jeanson

Since Specialization

Citations

This map shows the geographic impact of Ludovic Jeanson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ludovic Jeanson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ludovic Jeanson more than expected).

Fields of papers citing papers by Ludovic Jeanson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ludovic Jeanson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ludovic Jeanson. The network helps show where Ludovic Jeanson may publish in the future.

Co-authorship network of co-authors of Ludovic Jeanson

This figure shows the co-authorship network connecting the top 25 collaborators of Ludovic Jeanson. A scholar is included among the top collaborators of Ludovic Jeanson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ludovic Jeanson. Ludovic Jeanson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Jeanson, Ludovic, Lucie Thomas, Bruno Copin, et al.. (2016). Mutations inGAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization. Human Mutation. 37(8). 776–785. 41 indexed citations

2.

Jeanson, Ludovic, Bruno Copin, Jean‐François Papon, et al.. (2015). RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes. The American Journal of Human Genetics. 97(1). 153–162. 66 indexed citations

3.

Jeanson, Ludovic, Ida Chiara Guerrera, Jean‐François Papon, et al.. (2014). Proteomic Analysis of Nasal Epithelial Cells from Cystic Fibrosis Patients. PLoS ONE. 9(9). e108671–e108671. 23 indexed citations

4.

Nguyen‐Khoa, Thao, Cérina Chhuon, Ludovic Jeanson, et al.. (2014). A New Workflow for Proteomic Analysis of Urinary Exosomes and Assessment in Cystinuria Patients. Journal of Proteome Research. 14(1). 567–577. 38 indexed citations

5.

Kott, Esther, Philippe Duquesnoy, Bruno Copin, et al.. (2012). Loss-of-Function Mutations in LRRC6 , a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 91(5). 958–964. 124 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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